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Laser Synthesis and Luminescence Properties of SrAl2O4 ... - CSIC

Laser Synthesis and Luminescence Properties of SrAl2O4 ... - CSIC

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greenish emission is attributed to Eu 2+ located inside the host lattice. The width <strong>of</strong> the<br />

b<strong>and</strong>s confirms this result as it is due to the splitting <strong>of</strong> the mixed 4f5d state by the<br />

crystal field <strong>of</strong> the host lattice. Furthermore, no emission peaks in the red region from<br />

the characteristic intraconfigurational transition 4f → 4f <strong>of</strong> Eu 3+ have been detected,<br />

indicating that the rare earth ions that have not diffused remain as divalent europium<br />

ions in the grain boundaries. Here, their concentration is so high in comparison to the<br />

reduced area <strong>of</strong> grain boundaries, that the emission from these Eu 2+ ions could be<br />

largely quenched, resulting in shorter lifetime values than those corresponding to Eu 2+<br />

ions located inside the grains. On the other h<strong>and</strong>, the wavelength <strong>of</strong> the emission b<strong>and</strong><br />

does not vary from <strong>SrAl2O4</strong>:Eu 2+ to <strong>SrAl2O4</strong>: Eu 2+ , Dy 3+ . The luminescent centers are<br />

Eu 2+ ions, <strong>and</strong> no additional emission b<strong>and</strong> assigned to Dy 3+ is found in <strong>SrAl2O4</strong>: Eu 2+ ,<br />

Dy 3+ . As expected, only the phosphors co-doped with Dy 3+ exhibit significant long-<br />

lasting afterglow properties. 2<br />

Decay curves <strong>of</strong> the afterglow <strong>of</strong> <strong>SrAl2O4</strong>:Eu 2+ <strong>and</strong> <strong>SrAl2O4</strong>: Eu 2+ , Dy 3+ samples<br />

at room temperature are depicted in Fig. 10. The luminescence decay process <strong>of</strong> the<br />

samples is nonexponential. Both decay processes <strong>of</strong> luminescence undergo an initial<br />

fast decay (not shown), followed by a slow decaying process which accounts for the<br />

observed long-lasting phosphorescence. The fast decay process corresponds to the<br />

intrinsic lifetime <strong>of</strong> Eu 2+ . The slower decay process, which is significant only in<br />

<strong>SrAl2O4</strong>: Eu 2+ , Dy 3+ samples, is attributed to the presence <strong>of</strong> Dy 3+ ions into the host<br />

lattice.<br />

The measured luminescent properties <strong>of</strong> the phosphors synthesized by this novel<br />

laser melting method can be explained in terms <strong>of</strong> the thermally-activated hole trapping<br />

<strong>and</strong> detrapping mechanism proposed by Matsuzawa et al. 2,31 Based on it, the Dy 3+ ions<br />

act as deep hole trapping centers. Upon UV-light exposure, Eu 2+ excitation occurs as a

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